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Triple Test (2 nd Trimester) Test
Blood Test
For Female
NABL Certified
The triple test, also called triple screen, the Kettering test or the Bart's test, is an investigation performed during pregnancy in the second trimester to classify a patient as either high-risk or low-risk for chromosomal abnormalities (and neural...
Fasting is not required for this test.
About This Test
The triple test, also called triple screen, the Kettering test or the Bart's test, is an investigation performed during pregnancy in the second trimester to classify a patient as either high-risk or low-risk for chromosomal abnormalities (and neural tube defects). The triple marker screen test analyzes how likely an unborn baby is to have certain genetic disorders. It is also known as a multiple marker test. The exam measures the levels of three important substances in the placenta: alpha-fetoprotein (AFP), human chorionic gonadotropin (HCG), and estriol. The results of the triple marker screen test show the likelihood of an infant having a genetic disorder such as Down syndrome or spina bifida.
Triple Test (2 nd Trimester)
Birth defects
Birth Defect-Delay in meeting developmental milestones, feeding Problem, difficulty in breathing, failed newborn hearing test, seizures.
Triple Test (2 nd Trimester) Test
✅ Free home sample collection in all cities
✅ NABL & NABH certified lab partners
✅ Full refund if cancelled before sample collection
✅ Reports delivered on WhatsApp & Email
Why You Need Triple Test (2 nd Trimester) Test
The Triple Test (2 nd Trimester) Test is a blood test test designed for female aged All Ages. It helps in early detection and monitoring of health conditions. Book from NABL-certified labs.
What This Test Measures
The triple test, also called triple screen, the Kettering test or the Bart's test, is an investigation performed during pregnancy in the second trimester to classify a patient as either high-risk or low-risk for chromosomal abnormalities (and neural tube defects). The triple marker screen test analyzes how likely an unborn baby is to have certain genetic disorders. It is also known as a multiple marker test. The exam measures the levels of three important substances in the placenta: alpha-fetoprotein (AFP), human chorionic gonadotropin (HCG), and estriol. The results of the triple marker screen test show the likelihood of an infant having a genetic disorder such as Down syndrome or spina bifida.
Conditions Detected
Birth defects
When Should You Get This Test?
Birth Defect-Delay in meeting developmental milestones, feeding Problem, difficulty in breathing, failed newborn hearing test, seizures.
How It Works — Simple 3-Step Process
Step 1: Choose your preferred NABL-certified lab and select your appointment date.
Step 2: A trained phlebotomist visits your home at your chosen time for sample collection — completely free.
Step 3: Receive your detailed digital reports within 3 days on WhatsApp and email.
Medically Reviewed & Clinically Validated
This test follows ICMR (Indian Council of Medical Research) guidelines for diagnostic testing in adults aged All Ages. All tests are conducted at NABL and NABH accredited laboratories with internationally calibrated equipment.
Medically reviewed by the PrognoHealth Clinical Advisory Team
What Our Customers Say
Verified reviews from customers who booked Triple Test (2 nd Trimester) Test with PrognoHealth.
Frequently Asked Questions
Everything you need to know about Triple Test (2 nd Trimester) Test.
What is Triple Test (2 nd Trimester) Test?
The triple test, also called triple screen, the Kettering test or the Bart's test, is an investigation performed during pregnancy in the second trimester to classify a patient as either high-risk or low-risk for chromosomal abnormalities (and neural tube defects). The triple marker screen test analyzes how likely an unborn baby is to have certain genetic disorders. It is also known as a multiple marker test. The exam measures the levels of three important substances in the placenta: alpha-fetoprotein (AFP), human chorionic gonadotropin (HCG), and estriol. The results of the triple marker screen test show the likelihood of an infant having a genetic disorder such as Down syndrome or spina bifida.
Is home sample collection available for this test?
Yes, free home sample collection is available in all supported cities. A trained phlebotomist will visit your home at your preferred time to collect samples.
Do I need to fast before this test?
Not Required. Please follow any instructions given at the time of booking.
How long does it take to get the reports?
Digital reports are delivered within 3 days of sample collection via WhatsApp and email.
Can I cancel my booking and get a refund?
Yes, a full refund is provided if cancelled before sample collection. Once sample collection has been initiated, cancellation and refund are not possible. Contact PrognoHealth support at +91 9510650660 for assistance.
Easy Refund Policy
Cost free sample pickup from Home or Office.
Cancel before collection — full refund within 24 hours.
Reschedule appointment — no charges levied.
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